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This may adversely affect ventilation by causing deterioration of respiratory function and making ventilation less efficient. These problems do not occur with thoracoscopic DP (TDP), since the lower intercostal muscles are left intact. 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Am J Emerg Med 6:137–142\nMalhotra S, Roth DA, Gouge TH, Hofstetter SR, Sidhu G, Newman E (1998) Gangrene of Meckel’s diverticulum secondary to axial torsion: a rare complication. Am J Gastroenterol 93:1373–1375\nLee KH, Yeung CK, Tam YH, Ng WT, Yip KF (2000) Laparascopy for definitive diagnosis and treatment of gastrointestinal bleeding of obscure origin in children. J Pediatr Surg 35:1291–1293\nLoh DL, Munro FD (2003) The role of laparoscopy in the management of lower gastro-intestinal bleeding. Pediatr Surg Int 19:266–267\nSanders LE (1995) Laparoscopic treatment of Meckel’s diverticulum. Obstruction and bleeding managed with minimal morbidity. Surg Endosc 9:724–727\nSwaniker F, Soldes O, Hirschl RB (1999) The utility of technetium 99 m pertechnetate scintigraphy in the evaluation of patients with Meckel’s diverticulum. J Pediatr Surg 34:760–764\nTeitelbaum DH, Polley TZ Jr, Obeid F (1994) Laparoscopic diagnosis and excision of Meckel’s diverticulum. J Pediatr Surg 29:495–497\nTashjian DB, Moriarty KP (2003) Laparoscopy for treating a small bowel obstruction due to a Meckel’s diverticulum. JSLS 7:253–255\nAttwood SE, McGrath J, Hill AD, Stephens RB (1992) Laparoscopic approach to Meckel’s diverticulectomy. Br J Surg 79:211\nNg WT, Wong MK, Kong CK, Chan YT (1992) Laparoscopic approach to Meckel’s diverticulectomy. Br J Surg 79:973–974\nAltinli E, Pekmezci S, Gorgun E, Sirin F (2002) Laparoscopy-assisted resection of complicated Meckel’s diverticulum in adults. Surg Laparosc Endosc Percutan Tech 12:190–194\nPrasad TR, Chui CH, Jacobsen AS (2006) Laparoscopic-assisted resection of Meckel’s diverticulum in children. JSLS 10:310–316\nSchier F, Hoffmann K, Waldschmidt J (1996) Laparoscopic removal of Meckel’s diverticula in children. Eur J Pediatr Surg 6:38–39\nHuang CS, Lin LH (1993) Laparoscopic Meckel’s diverticulectomy in infants: report of three cases. J Pediatr Surg 28:1486–1489\nShalaby RY, Soliman SM, Fawy M, Samaha A (2005) Laparoscopic management of Meckel’s diverticulum in children. J Pediatr Surg 40:562–567\nRothenberg SS (2002) Laparoscopic segmental intestinal resection. Semin Pediatr Surg 11:211–216\nPrasad TR, Chui CH, Jacobsen AS (2006) Laparoscopic resection of torted Meckel’s diverticulum in a 13-year-old boy. J Laparoendosc Adv Surg Tech A 16:425–427\nMukai M, Takamatsu H, Noguchi H, Fukushige T, Tahara H, Kaji T (2002) Does the external appearance of a Meckel’s diverticulum assist in choice of the laparoscopic procedure? Pediatr Surg Int 18:231–233\nMackey WC, Dineen P (1983) A fifty year experience with Meckel’s diverticulum. Surg Gynecol Obstet 156:56–64\nPark JJ, Wolff BG, Tollefson MK, Walsh EE, Larson DR (2005) Meckel diverticulum: the Mayo Clinic experience with 1476 patients (1950–2002). Ann Surg 241:529–533\nPrasad TR, Chui CH, Jacobsen AS (2006) Laparoscopic appendicectomy in children: a trainee’s perspective. Ann Acad Med Singapore 35:694–697\nCullen JJ, Kelly KA, Moir CR, Hodge DO, Zinsmeister AR, Melton LJ III (1994) Surgical management of Meckel’s diverticulum. An epidemiologic, population-based study. Ann Surg 220:564–569\nCullen JJ, Kelly KA (1996) Current management of Meckel’s diverticulum. Adv Surg 29:207–214\nAmoury RA, Snyder CL (1998) Meckel’s diverticulum. In: O’Neill JA, Rowe MI, Grosfeld JL, Fonkalsrud EW, Coran AG (eds) Pediatric Surgery, Mosby, St. Louis, pp 1173–1184",{"EN":204},"",{"EN":206},"Meckel’s diverticulum (MD), a seemingly innocuous anomaly of the gastrointestinal tract, presents distinctive challenges to a clinician, as it is prone to varied complications that are frequently elusive to diagnosis with conventional diagnostic modalities. This case series illustrates the diverse presentations and advantages of laparoscopic-assisted management of Meckel’s diverticular complications in children. Between October 2002 and April 2006, 36 patients (27 males and 9 females) aged 1.5 to 16 years (median 10 years) underwent laparoscopic-assisted trans-umbilical Meckel’s diverticulectomy (LATUM). Sixteen (44.4%) patients presented with lower gastrointestinal bleeding (14 with painless bleed and 2 with perforated peptic ulcer in the ileum adjacent to the MD), six (16.7%) patients presented with intestinal obstruction (four due to a mesodiverticular band and one each due to intussusception and floppy giant cystic dilatation of MD causing intestinal compression) and four (11.1%) patients presented with features masquerading as appendicitis (one with Meckel’s diverticulitis and perforation, one with perforated peptic ulcer adjacent to MD and two with a torted and gangrenous MD). In ten (27.8%) patients, incidental MD with a narrow base was noted at laparoscopic exploration for suspected appendicitis. All patients underwent successful LATUM along with appendicectomy in 15 (41.7%) patients. The operative duration ranged from 72 to 266 min (mean 125.9 ± 48.4). There were no intra-operative complications and none required conversion to open surgery. The hospital stay was 3 to 9 days (mean 5.3 ± 1.2). There were three (8.3%) cases of postoperative adhesive intestinal obstruction; two underwent successful laparoscopic adhesiolysis and one necessitated conversion to suprapubic laparotomy to release the pelvic adhesions. There were no other complications during the follow-up (median 16 months). LATUM is a safe, effective and an esthetic procedure offering timely diagnosis and cure for diverse Meckel’s diverticular complications. 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Radiology 108: 665–666\nBergmann M, Charnas RM (1958) Tracheobronchial rests in the esophagus. J Thorac Surg 35: 97–102\nBluestone CD, Kerry R, Sieber WK (1969) Congenital esophageal stenosis. Laryngoscope 79: 1095–1104\nBonilla KB, Bowers WF (1959) Congenital esophageal stenosis; pathologic studies following resection. Am J Surg 97: 772–776\nBriceno LI, Grases PJ, Gallego S (1981) Tracheobronchial and pancreatic remnants causing esophageal stenosis. J Pediatr Surg 16: 731–732\nBuck P, Berger P, Sauvage P, El Mejjati A, Horber R (1971) Sténose congénitale de l'oesophage par dysgénésie trachéobronchique. Ann Chir Inf 12: 249–252\nChavrier Y, Lavras B, Gerard JB, Freycon F (1974) Sténose congénitale de l'oesophage chez un enfant d'un an. Pédiatrie 29: 527–531\nDeiraniya AK (1974) Congenital esophageal stenosis due to tracheobronchial remnants. Thorax 29: 720–725\nFonkalsrud EW (1972) Esophageal stenosis due to tracheobronchial remnants. Am J Surg 124: 101–103\nHuchzermeyer H, Burdelski M, Hruby M (1979) Endoscopic therapy of a congenital oesophageal stricture. Endoscopy 4: 259–262\nIbrahim NB, Sandry RJ (1981) Congenital oesophageal stenosis caused by tracheobronchial structures in the oesophageal wall. Thorax 36: 465–468\nIshida M, Tsuchida Y, Saito S (1969) Congenital esophageal stenosis due to tracheobronchial remnants. J Pediatr Surg 4: 339–345\nKluth D (1976) Atlas of esophageal atresia. J Pediatr Surg 11: 901–918\nKumar R (1962) A case of congenital oesophageal stricture due to a cartilaginous ring. Br J Surg 69: 533–534\nLongstreth GF, Wolochow DA, Tu RT (1979) Double congenital midesophageal webs in adults. Dig Dis Sci 24: 162–165\nMahour GH, Johnston PW, Gwinn JL, Hays D (1971) Congenital esophageal stenosis distal to esophageal atresia. Surgery 69: 936–939\nMoyson F (1970) Sténose oesophagienne congénitale et fistule trachéo-oesophagienne cervicale. Ann Chir Inf 11: 179–183\nMyers NA, Aberdeene E, Randolph J Pediatric surgery 3rd edn. Year Book Medical Publishers, pp. 469–472\nNishina T, Tsuchida Y, Saitos (1981) Congenital esophageal stenosis due to tracheobronchial remnants and its associated anomalies. J Pediatr Surg 16: 190–193\nNuyts JP, Piquet JJ, Bombart E, Lejeune M, Ryckwaert P (1971) Sténose congénitale de l'oesophage. A propos de deux observations. Pédiatrie 26: 243–249\nOhkawa H, Takahashi H, Hoshino Y, Sato H (1975) Lower esophageal stenosis in association with tracheobronchial remnants. J Pediatr Surg 10: 453–457\nOverton RC, Creech O (1958) Unusual esophageal atresia with distant membranous obstruction of the esophagus. J Thoracic Surg 35: 674–677\nPaulino F, Roselli A, Aprigliano F (1963) Congenital esophageal stricture due to tracheobronchial remnants. Surgery 53: 547–550\nPetit P, Borde J, Gubler JP, Touraine P (1970) Les rétrécissements congénitaux de l'oesophage. Ann Chir Inf 11: 153–170\nRose JS, Kassner EG, Jurgens KH, Farman J (1975) Congenital oesophageal strictures due to cartilaginous rings. Br J Radiology 48: 16–18\nRossier A, De Montis G, Chabrolle JP (1977) Congenital oesophageal stenosis and herpes simplex infection. Arch Dis Child 52: 982\nSchwartz SI (1962) Congenital membranous obstruction of esophagus. Arch Surg 85: 480–482\nSneed WF, Lagarde DC, Kogutt MS, Arensman RM (1979) Esophageal stenosis due to cartilaginous tracheobronchial remnants. J Pediatr Surg 14: 786–788\nSoave F, Mezzano A (1965) Kongenitale Ösophagusstenose durch Knorpeleinschlüsse in der Wand. Z Kinderchir 2: 487–492\nSpitz L (1973) Congenital esophageal stenosis distal to associated esophageal atresia. J Pediatr Surg 8: 973–974\nSteiner E, Scharfetter H, Gschnitzer F (1978) Bericht über 4 Fälle von Kongenitaler Ösophagenstenose. Wien Med Wochenschrift 128: 517–519\nStephens HB (1970) H-type tracheoesophageal fistula complicated by esophageal stenosis. 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J Pediatr Gastroenterol Nutr 37(1):4–21\nMcKiernan PJ, Baker AJ, Kelly DA (2000) The frequency and outcome of biliary atresia in the UK and Ireland. Lancet 355(9197):25 –29\nKarrer FM et al (1990) Biliary atresia registry, 1976 to 1989. J Pediatr Surg 25\nChardot C (2006) Biliary atresia. Orphanet J Rare Dis 1:28\nLivesey E et al (2009) Epidemiology of biliary atresia in England and Wales (1999–2006). Arch Dis Child Fetal Neonatal Ed 94(6):F451-F455\nHsiao CH et al (2008) Universal screening for biliary atresia using an infant stool color card in Taiwan. Hepatology 47(4):1233–1240\nNio M et al (2003) Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese Biliary Atresia Registry. J Pediatr Surg 38(7):997–1000\nCheng G et al (2013) Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. J Hepatol 59(6):1285–1291\nKarrer FM et al (1990) Biliary atresia registry, 1976 to 1989. J Pediatr Surg 25(10):1076–1080\nKasai M, Suzuki S (1959) A new operation for non-correctable biliary atresia—hepatic portoenterostomy. Shujutsu 13:733–739\nNio M et al (2006) Long-term outcome in type I biliary atresia. J Pediatr Surg 41(12):1973–1975\nSuperina R et al (2011) The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 254(4):577–585\nChardot C et al (1999) Prognosis of biliary atresia in the era of liver transplantation: French national study from 1986 to 1996. Hepatology 30(3):606–611\nBalistreri WF et al (1996) Biliary atresia: current concepts and research directions. Summary of a symposium. Hepatology 23(6):1682–1692\nOtte JB et al (1994) Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: a review. Hepatology 20(1 Pt 2):41S–48S\nEngelmann G et al (2007) Indications for pediatric liver transplantation. Data from the Heidelberg pediatric liver transplantation program. Nephrol Dial Transpl 22(suppl 8):viii23-viii28\nShneider BL et al (2006) A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr 148(4):467–474\nShneider BL, Mazariegos GV (2007) Biliary atresia: a transplant perspective. Liver Transpl 13(11):1482–1495\nBessho K (2015) Complications and quality of life in long-term survivors of biliary atresia with their native livers. J Pediatr\nBijl EJ et al (2013) The long-term outcome of the Kasai operation in patients with biliary atresia: a systematic review. Neth J Med 71(4):170–173\nHoward ER et al (2001) Survival patterns in biliary atresia and comparison of quality of life of long-term survivors in Japan and England. J Pediatr Surg 36(6):892–897\nOkazaki T et al (1999) Long-term postsurgical outcome of biliary atresia. J Pediatr Surg 34(2):312–315\nLykavieris P et al (2005) Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver. Hepatology 41(2):366–371\nAltman RP et al (1997) A multivariable risk factor analysis of the portoenterostomy (Kasai) procedure for biliary atresia: twenty-five years of experience from two centers. Ann Surg 226(3):348–353 (discussion 353–355)\nde Vries W et al (2011) Twenty-year transplant-free survival rate among patients with biliary atresia. Clin Gastroenterol Hepatol 9(12):1086–1091\nNio M et al (1997) The outcome of surgery for biliary atresia and the current status of long-term survivors. Tohoku J Exp Med 181(1):235–244\nShinkai M et al (2009) Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a children’s hospital. J Pediatr Gastroenterol Nutr 48(4):443–450\nNg VL et al (2014) Medical status of 219 children with biliary atresia surviving long-term with their native livers: results from a North American multicenter consortium. J Pediatr 165(3):539–546 e2\nKumagi T et al (2012) Biliary atresia and survival into adulthood without transplantation: a collaborative multicentre clinic review. Liver Int 32(3):510–518\nBu LN et al (2003) Prophylactic oral antibiotics in prevention of recurrent cholangitis after the Kasai portoenterostomy. J Pediatr Surg 38(4):590–593\nLuo Y, Zheng S (2008) Current concept about postoperative cholangitis in biliary atresia. World J Pediatr 4(1):14–19\nLien TH et al (2015) Use of Lactobacillus casei rhamnosus to prevent cholangitis in biliary atresia after Kasai operation. J Pediatr Gastroenterol Nutr 60(5):654–658\nShneider BL et al (2012) Portal hypertension in children and young adults with biliary atresia. J Pediatr Gastroenterol Nutr 55(5):567–573\nAmitrano L et al (2012) The effectiveness of current acute variceal bleed treatments in unselected cirrhotic patients: refining short-term prognosis and risk factors. Am J Gastroenterol 107(12):1872–1878\nAugustin S et al (2011) Effectiveness of combined pharmacologic and ligation therapy in high-risk patients with acute esophageal variceal bleeding. Am J Gastroenterol 106(10):1787–1795\nGarcia-Tsao G et al (2007) Prevention and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology 46(3):922–938\nFagundes ED et al (2008) Clinical and laboratory predictors of esophageal varices in children and adolescents with portal hypertension syndrome. J Pediatr Gastroenterol Nutr 46(2):178–183\nGana JC et al (2011) A clinical prediction rule and platelet count predict esophageal varices in children. Gastroenterology 141(6):2009–2016\nAdami MR et al (2013) Noninvasive methods for prediction of esophageal varices in pediatric patients with portal hypertension. World J Gastroenterol 19(13):2053–2059\nKlein GL et al (2002) Hepatic osteodystrophy in chronic cholestasis: evidence for a multifactorial etiology. Pediatr Transpl 6(2):136–140\nGoda T et al (2013) The most reliable early predictors of outcome in patients with biliary atresia after Kasai’s operation. J Pediatr Surg 48(12):2373–2377\nTomita H et al (2014) Long-term native liver fibrosis in biliary atresia: development of a novel scoring system using histology and standard liver tests. J Hepatol 60(6):1242–1248\nGupta S et al (2010) Improved survival after liver transplantation in patients with hepatopulmonary syndrome. Am J Transpl 10(2):354–363\nChen K, Li B (2011) Reversal of severe hepatopulmonary syndrome in chronic hepatic cirrhosis by living donor liver transplantation: report of two cases. Surg Today 41(3):441–443\nCartin-Ceba R, Krowka MJ (2014) Portopulmonary hypertension. Clin Liver Dis 18(2):421–438\nKrowka MJ, Wiesner RH, Heimbach JK (2013) Pulmonary contraindications, indications and MELD exceptions for liver transplantation: a contemporary view and look forward. J Hepatol 59(2):367–374\nAyoub T (2011) Pulmonary hypertension in liver transplant. Curr Opin Organ Transpl 16(3):331–337\nVera A, Villaveces D, Lopez R (2012) Orthotopic liver transplantation for biliary atresia complicated by incidental cholangiocarcinoma. J Pediatr Gastroenterol Nutr 55(3):336–337\nHadzic N et al (2011) Hepatocellular carcinoma in biliary atresia: King’s College Hospital experience. J Pediatr 159(4):617–622 e1\nSundaram SS et al (2013) Health related quality of life in patients with biliary atresia surviving with their native liver. J Pediatr 163(4):1052-7 e2\nLee WS, Ong SY (2016) Health-Related Quality of Life in Children with Biliary Atresia Living with Native Livers. Ann Acad Med Singapore 45(2):61–68\nLind RC et al (2015) Health status and quality of life in adult biliary atresia patients surviving with their native livers. Eur J Pediatr Surg 25(1):60–65",{"VI":641,"EN":642},"Tắc mật bẩm sinh (Biliary atresia - BA) là một căn bệnh tắc nghẽn mật hiếm gặp ở trẻ sơ sinh, dẫn đến bệnh lý tắc mật và tắc nghẽn ống mật tiến triển, gây ra hiện tượng tắc mật và vàng da. Phương pháp phẫu thuật tiêu chuẩn là phẫu thuật hepatoportoenterostomy (phẫu thuật Kasai). Mặc dù khoảng 50% trẻ sơ sinh bị ảnh hưởng sẽ cần ghép gan trong 2 năm đầu đời, nhưng 50% còn lại có thể sống nhiều năm với gan tự nhiên của họ, mặc dù có sự tiến triển của xơ gan và bệnh gan mãn tính. Nhiều bệnh nhân trong số này sẽ gặp phải các biến chứng lâu dài như nhiễm trùng đường mật tái phát, tăng huyết áp tĩnh mạch cửa, chảy máu từ giãn tĩnh mạch, vấn đề tăng trưởng, các bất thường sinh hóa, và bệnh lý xương liên quan đến gan. Những bệnh lý này gây ra một tác động lớn đến chất lượng cuộc sống của bệnh nhân và gia đình của họ. Trong bài báo này, chúng tôi thực hiện một đánh giá toàn diện về tình trạng lâm sàng và chất lượng cuộc sống của những người sống sót lâu dài sau khi phẫu thuật tắc mật bẩm sinh với gan tự nhiên, nhằm tạo điều kiện cho việc theo dõi kỹ lưỡng lâu dài các bệnh nhân này và cảnh báo các nhân viên chăm sóc sức khỏe về những biến chứng có thể xảy ra.","Biliary atresia (BA) is a rare neonatal cholestatic disease which leads to progressive obliterative cholangiopathy, resulting in biliary obstruction and jaundice. The standard surgical treatment is hepatoportoenterostomy (Kasai operation). Although approximately 50% of the affected infants would require liver transplantation within the first 2 years of life, the other 50% of the patients can live for years with their native liver, despite the progression of cirrhosis and chronic liver disease. Many of these patients will be affected by long-term complications such as repeated cholangitis, portal hypertension, variceal bleeding, growth problems, biochemical abnormalities, and hepatic osteodystrophy. These morbidities impose a huge impact on the quality of life of the patients and their families. Herein, we performed a comprehensive review on the clinical status and quality of life of long-term survivors of biliary atresia with their native livers, to facilitate meticulous longitudinal follow-up of these patients, and alert caregivers the probable complications to be aware of.",{"VI":644,"EN":645},"Tổng quan về kết quả lâu dài và chất lượng cuộc sống của bệnh nhân sau phẫu thuật Kasai sống với gan tự nhiên","A review of long-term outcome and quality of life of patients after Kasai operation surviving with native livers",{"VOID":647},"10.1007\u002Fs00383-017-4158-4",{"VI":649},"tắc mật bẩm sinh, phẫu thuật Kasai, gan tự nhiên, chất lượng cuộc sống, biến chứng lâu dài","2025-01-10T05:13:38.416+00:00",[652],"VI","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00383-017-4158-4",[655,670],{"id":656,"sortIndex":19,"researcher":18,"roles":657,"affiliations":658,"properties":667},"389369a9-e4e4-4c24-80d9-6fec6ccca901",[145],[659],{"id":18,"sortIndex":19,"affiliation":660,"properties":18},{"id":661,"createTime":662,"updateTime":662,"relativeEntities":663,"slug":18,"properties":664,"entityType":54,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"3672db01-bd88-4412-84b7-15ec8e160a9a","2024-02-18T02:31:31.473+00:00",[],{"title":665},{"VI":666},"Department of Surgery, Li Ka Shing Faculty of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China",{"title":668},{"VI":669},"Kenneth K. Y. Wong",{"id":671,"sortIndex":116,"researcher":18,"roles":672,"affiliations":673,"properties":679},"3b92cf5a-0580-476b-b8e4-67d7595c330c",[145],[674],{"id":18,"sortIndex":19,"affiliation":675,"properties":18},{"id":661,"createTime":662,"updateTime":662,"relativeEntities":676,"slug":18,"properties":677,"entityType":54,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},[],{"title":678},{"VI":666},{"title":680},{"VI":681},"Carol W. Y. Wong",{"url":653,"publisher":683,"properties":710},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":684,"slug":10,"properties":685,"entityType":16,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19,"subjectFields":688,"manageAffiliations":689,"indexDatabases":690,"url":110,"thumbnailPath":18,"statistic":705,"gsStatistic":18,"type":119,"analyzePriority":18},[],{"issn":686,"title":687},{"VOID":13},{"EN":15},[],[],[691,698],{"id":70,"indexDatabase":692,"url":83,"indexYears":84,"academicFieldIds":697,"indexDatabaseRanking":89},{"id":72,"createTime":73,"updateTime":74,"relativeEntities":693,"label":694,"description":695,"key":80,"publicationTags":696,"standard":18},[],{"EN":77,"VI":77},{"EN":77,"VI":79},[82],[86,87,88],{"id":91,"indexDatabase":699,"url":106,"indexYears":18,"academicFieldIds":704,"indexDatabaseRanking":18},{"id":93,"createTime":94,"updateTime":95,"relativeEntities":700,"label":701,"description":702,"key":102,"publicationTags":703,"standard":18},[],{"EN":98,"VI":98},{"VI":100,"EN":101},[104,105],[108,109],{"impactFactor":19,"impactFactorByYear":706,"i10Index":19,"i10IndexLast5Year":19,"totalPublication":113,"totalPublicationByYear":707,"totalCitation":19,"totalCitationByYear":708,"totalCitationPerPublication":19,"totalCitationPerPublicationByYear":709,"hindexLast5Year":19,"hindex":19},{},{"2023":115,"2024":116},{},{},{"volume":711,"pages":713},{"VOID":712},"33",{"VOID":714},"1283-1287","2017-09-22",2017,{"id":718,"createTime":719,"updateTime":720,"relativeEntities":721,"slug":722,"properties":723,"entityType":137,"verifyStatus":138,"verifyTime":720,"verifyNote":139,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":732,"fullTextUrl":18,"authors":733,"publicationType":158,"publisherRelationship":821,"citationCount":18,"citationInfo":18,"publishDate":854,"publishYear":855,"citationAnalyzeStatus":17,"lastCitationAnalyze":18,"indexDatabases":18,"openAccess":18,"references":18,"isForceReanalyzing":194},"a82ffb42-1046-433c-9162-e39b5c66ea2c","2024-01-03T11:57:08.914+00:00","2024-12-28T23:56:32.190+00:00",[],"Percutaneous-internal-ring-suturing-as-a-first-choice-laparoscopic-inguinal-hernia-repair-method-in-girls-a-single-center-study-in-148-patients",{"references":724,"abstract":726,"title":728,"doi":730},{"VOID":725},"Li C, Xu L, Peng Y, Liang X, Lin W (2015) Effects of single-port laparoscopic percutaneous extraperitoneal closure on the orientation of the vas deferens and testicular perfusion and volume: Experience from a single center. J Pediatr Urol. doi:10.1016\u002Fj.jpurol.2015.11.006\nBertozzi M, Marchesini L, Tesoro S, Appignani A (2015) Laparoscopic herniorrhaphy in children. Pediatr Med Chir 37(2):pmc.2015.109\nMontupet P, Esposito C (2011) Fifteen years experience in laparoscopic inguinal hernia repair in pediatric patients. Results and considerations on a debated procedure. Surg Endosc 25:450–453\nPatkowski D, Czernik J, Chrzan R (2006) Percutaneous internal ring suturing: a simple minimally invasive technique for inguinal hernia repair in children. J Laparoendosc Adv Surg Tech A 16:513–517\nShono T, Izaki T, Nakahori R, Yoshimaru K (2015) Testicular ascent after laparoscopic percutaneous extraperitoneal closure for inguinal hernias. Eur J Pediatr Surg 25:105–108\nXiang B, Jin S, Zhong L, Li F, Jiang X, Xu Z (2015) Reasons for recurrence after the laparoscopic repair of indirect inguinal hernia in children. J Laparoendosc Adv Surg Tech A. 25(8):681–683\nYildiz A, Çelebi S, Akin M et al (2012) Laparoscopic hernioraphy: a better approach for recurrent hernia in boys? Pediatr Surg Int 28:449–453\nWolak PK, Patkowski D (2014) Laparoscopic inguinal hernia repair in children using the percutaneous internal ring suturing technique—own experience. Wideochir Inne Tech Malo Inwazyjne 9:53–58\nKaradag CA, Erginel B, Sever N et al (2015) Laparoscopic hernia repair in children: which method is the best? J Exp Clin Med 33(1):11–13\nMontupet P, Esposito C (1999) Laparoscopic treatment of congenital inguinal hernia in children. J Pediatr Surg 34:420–423\nSchier F (1998) Laparoscopic herniorrhaphy in girls. J Pediatr Surg 33:1495–1497\nLi S, Li M, Wong KK, Liu L, Tam PK (2014) Laparoscopically assisted simple suturing obliteration (LASSO) of the internal ring using an epidural needle: a handy single-port laparoscopic herniorrhaphy in children. J Pediatr Surg 49:1818–1820\nYamoto M, Morotomi Y, Yamamoto M, Suehiro S (2011) Single-incision laparoscopic percutaneous extraperitoneal closure for inguinal hernia in children: an initial report. Surg Endosc 25:1531–1534\nTakehara H, Yakabe S, Kameoka K (2006) Laparoscopic percutaneous extraperitoneal closure for inguinal hernia in children: clinical outcome of 972 repairs done in 3 pediatric surgical institutions. J Pediatr Surg 41:1999–2003\nPatkowski D, Chrzan R, Jaworski W (2006) Percutaneous internal ring suturing for inguinal hernia repair in children under three months of age. Adv Clin Exp Med 15(5):851–856\nÇelebi S, Yıldız A, Üçgül A et al (2012) Do open repair and different laparoscopic techniques in pediatric inguinal hernia repairs affect the vascularization of testes? J Pediatr Surg 47:1706–1710\nChan KL, Chan HY, Tam PK (2007) Towards a near-zero recurrence rate in laparoscopic inguinal hernia repair for pediatric patients of all ages. J Pediatr Surg 42:1993–1997\nToufique Ehsan M, Ng AT, Chung PH et al (2009) Laparoscopic hernioplasties in children: the implication on contralateral groin exploration for unilateral inguinal hernias. Pediatr Surg Int 25:759–762\nEsposito C, Turial S, Alicchio F et al (2013) Laparoscopic repair of incarcerated inguinal hernia. A safe and effective procedure to adopt in children. Hernia 17:235–239\nThomas DT, Göcmen KB, Tulgar S, Boga I (2015) Percutaneous internal ring suturing is a safe and effective method for the minimal invasive treatment of pediatric inguinal hernia: experience with 250 cases. J Pediatr Surg 12:11",{"EN":727},"We sought to retrospectively assess the operative findings and clinical outcomes of 148 girls who underwent laparoscopic inguinal hernia repair with the percutaneous internal ring suturing (PIRS) technique. Between 2010 and 2014, girls with inguinal hernia underwent surgery using the laparoscopic PIRS technique described by Patkowski. Demographic and perioperative findings, complications, and recurrences were evaluated. A total of 205 inguinal hernia repairs were performed in 148 children with a mean age of 5.83 years (1 month–16 years). In 57 girls (38.5 %), the hernias were bilaterally repaired, while in 91 girls (61.5 %) hernias were unilaterally repaired. The mean follow-up time was 3.6 years (range 2.5–6.1 years). No serious complications or recurrence were noted. Granuloma occurred in one patient. The PIRS technique is a safe, simple and effective procedure for girls. Excellent cosmetic results and reduced recurrence rates are associated with this method. This procedure is particularly suitable for girls because they lack a spermatic cord and vascular structures that can cause complications with this technique in boys. Based on our experience and others in the literature, we suggest that the PIRS procedure might be considered a gold standard for inguinal hernia operations in girls.",{"EN":729},"Percutaneous internal ring suturing as a first choice laparoscopic inguinal hernia repair method in girls: a single-center study in 148 patients",{"VOID":731},"10.1007\u002Fs00383-016-3903-4","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00383-016-3903-4",[734,749,761,773,785,809],{"id":735,"sortIndex":257,"researcher":18,"roles":736,"affiliations":737,"properties":746},"2b0b0455-17db-4fa7-ab8d-2cdf9dc446b7",[145],[738],{"id":18,"sortIndex":19,"affiliation":739,"properties":18},{"id":740,"createTime":741,"updateTime":741,"relativeEntities":742,"slug":18,"properties":743,"entityType":54,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"92d8c326-9d17-4ae5-89c6-f78b2bbda91a","2024-01-03T11:57:08.991+00:00",[],{"title":744},{"VI":745},"Department of Pediatric Surgery, Sisli Etfal Education and Research Hospital, Istanbul, Turkey",{"title":747},{"VI":748},"Ali Ihsan Dokucu",{"id":750,"sortIndex":115,"researcher":18,"roles":751,"affiliations":752,"properties":758},"39ff4759-e09f-4889-856b-ae9741dee5bd",[145],[753],{"id":18,"sortIndex":19,"affiliation":754,"properties":18},{"id":740,"createTime":741,"updateTime":741,"relativeEntities":755,"slug":18,"properties":756,"entityType":54,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},[],{"title":757},{"VI":745},{"title":759},{"VI":760},"Cetin Ali 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JB (2012) The enteric nervous system and neurogastroenterology. Nat Rev Gastroenterol Hepatol 9(5):286–294\nBurns AJ (2005) Migration of neural crest-derived enteric nervous system precursor cells to and within the gastrointestinal tract. Int J Dev Biol 49(2–3):143–150\nGoldstein AM, Hofstra RM, Burns AJ (2013) Building a brain in the gut: development of the enteric nervous system. Clin Genet 83(4):307–316\nGranström AL, Danielson J, Husberg B et al (2015) Adult outcomes after surgery for Hirschsprung’s disease: evaluation of bowel function and quality of life. J Pediatr Surg 50(11):1865–1869\nZimmer J, Tomuschat C, Puri P (2016) Long-term results of transanal pull-through for Hirschsprung’s disease: a meta-analysis. Pediatr Surg Int 32(8):743–749\nSood S, Lim R, Collins L et al (2018) The long-term quality of life outcomes in adolescents with Hirschsprung disease. J Pediatr Sur 53(12):2430–2434\nBurns AJ et al (2016) White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies. Dev Biol 417(2):229–251\nHotta R, Cheng L, Graham HK et al (2016) Delivery of enteric neural progenitors with 5-HT4 agonist-loaded nanoparticles and thermosensitive hydrogel enhances cell proliferation and differentiation following transplantation in vivo. Biomaterials 88:1–11\nLindley RM, Hawcutt DB, Connell MG et al (2009) Properties of secondary and tertiary human enteric nervous system neurospheres. J Pediatr Surg 44(6):1249–1255\nFattahi F, Steinbeck JA, Kriks S et al (2016) Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease. Nature 531(7592):105–109\nZuber SM, Grikscheit TC (2019) Stem cells for babies and their surgeons: The future is now. J Pediatr Surg 54(1):16–20\nIannaccone PM et al (1994) Pluripotent embryonic stem cells from the rat are capable of producing chimeras. Dev Biol 163(1):288–292\nGiles JR, Yang X, Mark W et al (1993) Pluripotency of cultured rabbit inner cell mass cells detected by isozyme analysis and eye pigmentation of fetuses following injection into blastocysts or morulae. Mol Reprod Dev 36(2):130–138\nNotarianni E, Laurie S, Moor M et al (1990) Maintenance and differentiation in culture of pluripotential embryonic cell lines from pig blastocysts. J Reprod Fertil Suppl 41:51–56\nHandyside A, Hooper ML, Kaufman MH (1987) Towards the isolation of embryonal stem cell lines from the sheep. Rouxs Arch Dev Biol 196(3):185–219\nThomson JA et al (1998) Embryonic stem cell lines derived from human blastocyst. Science 282(5391):1145–1147\nKanda A et al (2012) Establishment of ES cells from inbred strain mice by dual inhibition (2i). J Reprod 58(1):77–83\nBondurand N, Sham MH (2013) The role of SOX10 during enteric nervous system development. Dev Biol 382(1):330–343\nShibata S, Yasuda A, Renault-Mihara F et al (2010) Sox10-Venus mice: a new tool for real-time labeling of neural crest lineage cells and oligodendrocytes. Mol Brain 3:31\nFujiwara N, Miyahara K, Nakazawa-Tanaka N et al (2016) Altered differentiation of enteric neural crest-derived cells from endothelin receptor-B null mouse model of Hirschsprung’s disease. Pediatr Surg Int 32(12):1095–1101\nBuehr M et al (2003) Genesis of embryonic stem cells. Philos Trans R Soc Lond B Biol Sci 358(1436):1397–1402\nYing QL, Wray J, Nichols J et al (2008) The ground state of embryonic stem cell self-renewal. Nature 453(7194):519–523\nFujiwara N, Miyahara K, Nakazawa-Tanaka N et al (2022) In vitro investigation of the differentiation of enteric neural crest-derived cells following transplantation of aganglionic gut in a mouse model. Pediatr Surg Int 38(5):755–759\nKawaguchi J, Nichols J, Gierl MS et al (2010) Isolation and propagation of enteric neural crest progenitor cells from mouse embryonic stem cells and embryos. Development 137:693–704\nYing QL, Smith AG (2003) Defined conditions for neural commitment and differentiation. Methods Enzymol 365:327–341\nAoki Y, Saint-Germain N, Gyda M (2003) Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. Dev Biol 259(1):19–33\nBondurand N, Kobetz A, Pingault V (1998) Expression of the SOX10 gene during human development. FEBS Lett 432(3):168–172\nStavely R, Bhave S, Ho WLN (2021) Enteric mesenchymal cells support the growth of postnatal enteric neural stem cells. Stem Cells 39(9):1236–1252\nObermayr F, Seitz G (2018) Recent developments in cell-based ENS regeneration – a short review. Innov Surg Sci 3(2):93–99\nMueller JL, Goldstein AM (2022) The science of Hirschsprung disease: what we know and where we are headed. Semin Pediatr Surg 31(2):151157\nRajabzadeh N, Fathi E, Farahzadi R (2019) Stem cell-based regenerative medicine. Stem Cell Investig 18(6):19\nHagl CI, Rauch U, Klotz M (2012) The microenvironment in the Hirschsprung’s disease gut supports myenteric plexus growth. Int J Colorectal Dis 27(6):817–829",{"EN":866},"Failure of enteric neural crest-derived cells (ENCCs) to correctly colonize the embryonic gut results in Hirschsprung’s disease (HD). Embryonic stem cells (ESCs) have the potential to differentiate into all tissue-specific cells and lineages, including ENCCs. We investigated the cellular differentiation of ESCs from Sox10-Venus + mice into both control and endothelin receptor-B knockout (Ednrb KO) mouse gut to assess each region. We established ESCs from Sox10-Venus + mice. These cells were cultured for 2 days, then selected and co-cultured with either a dissociated control or Sox10-Venus – Ednrb KO mouse gut (both small intestine and colon) on embryonic day (E) 13.5. Four days later, cells were immunolabeled for Tuj1 and visualized using confocal microscopy. Confocal microscopy revealed that transplanted Sox10-Venu + cells from ESCs migrated extensively within the host gut. Moreover, Tuj1-positive neurites were detected in the transplanted ESCs. Tuj1 expression was significantly decreased in aganglionic HD colon compared to controls (p \u003C 0.05) and the HD small intestine (p \u003C 0.05). This study demonstrated that an appropriate host environment is crucial for normal and complete colonization of the gut. 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Eur J Pediatr 145: 211–216\nMantor PC, Tugle DW, Tunell WP (1989) An appropriate negative bronchoscopy rate in suspected foreign body aspiration. Am J Surg 158: 622–624\nMu L, He P, Sun D (1991) Inhalation of foreign bodies in Chinese children: a review of 400 cases. Laryngoscope 101: 657–660\nSteen CH, Zimmermann T (1989) Tracheobronchial foreign body aspiration in children. Report of over 94 patients. Monatsschr Kinderheilkd 137: 138–143\nTeixidor-de-Otto J, Negro F, Gutierrez C (1980) Removal of foreign bodies from the upper airways and the bronchial tree of small children. Z Kinderchir Grenzgeb 30: 137–140\nWunderlich P, Dietzsch HJ, Leupold W, Burkardt J, Wehner J (1988) Acute foreign body aspiration as a respiratory emergency in childhood. Pediatr Pathol 23:223–232",{"EN":1089},"Foreign-body (FB) aspirations account for a reasonable percentage of respiratory emergencies in young children. 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